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Related Concept Videos

Scanning Electron Microscopy01:07

Scanning Electron Microscopy

A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
Overview of Electron Microscopy01:25

Overview of Electron Microscopy

The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been developed.
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...

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Related Experiment Video

Updated: May 28, 2026

Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals
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Scanning electron microscope image enhancement using spread spectrum through dither signal imposition.

Kwang Oh Jung1, Wonjong Joo, Dong Hwan Kim

  • 1Graduate School of NID Fusion Technology, Seoul National University of Science and Technology, Seoul 139-743, South Korea.

Journal of Electron Microscopy
|October 13, 2011
PubMed
Summary
This summary is machine-generated.

Minimizing noise in scanning microscopes is crucial for clear nanoscale imaging. This study introduces a dither signal injection method using spread spectrum techniques to reduce scan control circuit noise and enhance image quality.

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Area of Science:

  • Microscopy
  • Image Processing
  • Signal Analysis

Background:

  • Scanning electron microscopy is vital for nanoscale measurements.
  • Image noise, particularly from scan control circuits, degrades image clarity and resolution.
  • Existing methods struggle to effectively mitigate this specific type of noise.

Purpose of the Study:

  • To develop and validate a novel method for reducing image noise in scanning microscopes.
  • To improve the quality and clarity of images obtained at the nanoscale.
  • To address the limitations of current noise reduction techniques in scan control circuits.

Main Methods:

  • Implementation of dither signal injection into the scanning signal.
  • Utilizing spread spectrum techniques to manage noise originating from scan control circuits.
  • Processing secondary electron signals through a photomultiplier tube and analog-to-digital conversion.

Main Results:

  • Significant reduction in noise artifacts originating from the scan control circuit.
  • Demonstrated improvement in image clarity and detail for nanoscale samples.
  • Validation of the dither signal injection method's effectiveness.

Conclusions:

  • Dither signal injection combined with spread spectrum methods offers an effective solution for noise reduction in scanning microscopy.
  • This technique enhances the reliability of nanoscale measurements by improving image quality.
  • The proposed method presents a practical advancement for high-resolution imaging applications.